为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The spatial distribution of immune cell subpopulations in hepatocellular carcinoma.
The spatial distribution of immune cell subpopulations in hepatocellular carcinoma.
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肿瘤微环境(TME)中的浸润免疫细胞影响肿瘤进展和患者预后,使其成为免疫治疗研究中有吸引力的治疗靶点。需要更深入地了解肝细胞癌(HCC)TME中免疫细胞的分布,以识别可能影响潜在免疫治疗有效性的不同免疫细胞类型之间的相互作用。
我们使用来自302例HCC患者样本的组织微阵列进行多重免疫组织化学,以阐明HCC和正常肝组织中免疫细胞亚群(CD3+、CD4+、CD8+、CD66b+和CD68+)的空间分布。
我们使用Pearson相关性分析不同免疫亚群之间的关联。应用G(r)函数、K(r)函数和欧几里得距离来表征免疫细胞类型之间的双变量分布模式。使用Cox回归和Kaplan-Meier分析评估不同免疫细胞的肿瘤浸润与根治性手术后患者结局之间的关联。
我们还分析了不同免疫细胞亚群的空间分布与HCC患者预后之间的关系。我们发现HCC TME中的免疫细胞空间分布具有异质性。我们的研究为HCC免疫治疗提供了理论基础。
Infiltrating immune cells in the tumor microenvironment (TME) influence tumor progression and patient prognosis, making them attractive therapeutic targets for immunotherapy research. A deeper understanding of immune cell distributions in the TME in hepatocellular carcinoma (HCC) is needed to identify interactions among different immune cell types that might impact the effectiveness of potential immunotherapies.
We performed multiplex immunohistochemistry using a tissue microarray of samples from 302 patients with HCC to elucidate the spatial distributions of immune cell subpopulations (CD3 + , CD4 + , CD8 + , CD66b + , and CD68 + ) in HCC and normal liver tissues.
We analyzed the associations between different immune subpopulations using Pearson's correlation. G(r) functions, K(r) functions and Euclidean distance were applied to characterize the bivariate distribution patterns among the immune cell types. Cox regression and Kaplan-Meier analysis were used to evaluate the associations between tumor infiltration by different immune cells and patient outcomes after curative surgery.
We also analyzed the relationship between the spatial distribution of different immune cell subpopulations with HCC patient prognosis.
We found that the immune cell spatial distribution in the HCC TME is heterogeneous.
Our study provides a theoretical basis for HCC immunotherapy.
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